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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53285Erstellt: 24. Oktober 2026

Hexane → Methyl 4-[2-(1,1-dimethyl-3-oxo-indan-5-yl)vinyl]benzoate

https://huagongshe.com/de/reaction/53285

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
EduktSodium BicarbonateHCID 516892—
EduktMethyl 4-ethenylbenzoateHCID 583124—
Edukt6-bromo-3,3-dimethyl-2,3-dihydro-1H-inden-1-oneHCID 10776365—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorTetrabutylammonium chloride hydrateHCID 16212273—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 4-[2-(1,1-dimethyl-3-oxo-indan-5-yl)vinyl]benzoateHCID 5433662270%

Reaktionsschritte

6-Bromo-3,3-dimethyl-indan-1-one (1.20 g, 5.02 mmol), methyl 4-vinylbenzoate (1.63 g, 10.0 mmol), palladium acetate (56 mg, 0.25 mmol), tetrabutylammonium chloride hydrate (1.53 g, 5.52 mmol ), and sodium bicarbonate (1.05 g, 12.6 mmol) were stirred in 10 mL of anhydrous N,N-dimethylformamide at 80°-100° C. for 8 hours. The mixture was diluted with water (100 mL), extracted with methylene chloride (50 mL×3). The combined extracts were dried over magnesium sulfate and evaporated. The residue was purified by flash chromatography (CH2Cl2 :hexane=1:1 to 1:0, then CH2Cl2 :EtOAc=10:1) to give 1.12 g (70% yield) of the title compound as a yellow solid; 1H-NMR (CDCl3) δ1.45 (s, 6H), 2.64 (s, 2H), 5.30 (s, 3H), 7.18 (d, J=16.5 Hz, 1H), 7.26 (d, J=16.5 Hz, 1H), 7.52 (d, J=8.1 Hz, 1H), 7.58 (d, J=8.5 Hz, 2H), 7.78 (d, J=1.7, 8.1 Hz, 1H), 7.86 (d, J=1.7 Hz, 1H), 8.05 (d, J=8.5 Hz, 2H); MS m/e 321 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05618839
Quelldatensatzuspto-grants-1997_04
ORD IDord-e894fad907b74d91b47cdd45f501a1db
Quellennotizuspto-grants-1997_04